Herein we report a Pd‐catalyzed dearomative methoxyallylation of 3‐nitroindoles with readily available allyl carbonates. Good yields (up to 86 %) and diastereoselectivity (up to >20:1 dr) are obtained for a wide range of substrates. The compa...
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https://www.riss.kr/link?id=O107829139
2021년
eng
1433-7851
1521-3773
SCI;SCIE;SCOPUS
학술저널
Angewandte Chemie international edition
22184-22188 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Herein we report a Pd‐catalyzed dearomative methoxyallylation of 3‐nitroindoles with readily available allyl carbonates. Good yields (up to 86 %) and diastereoselectivity (up to >20:1 dr) are obtained for a wide range of substrates. The compa...
Herein we report a Pd‐catalyzed dearomative methoxyallylation of 3‐nitroindoles with readily available allyl carbonates. Good yields (up to 86 %) and diastereoselectivity (up to >20:1 dr) are obtained for a wide range of substrates. The compatibility of gram‐scale synthesis and the relatively low catalyst loading (down to 1 mol % of [Pd]) enhance the practicality of this method. The kinetic experiments indicate that the rate‐determining step of this reaction is the nucleophilic attack of the alkoxide anion.
An intermolecular Pd‐catalyzed dearomative methoxyallylation of 3‐nitroindoles with readily available allyl carbonates was reported. Good yields (up to 86 %) and diastereoselectivity (up to >20:1 dr) are obtained for a wide range of substrates. The compatibility of gram‐scale synthesis and the relatively low catalyst loading (down to 1 mol % of [Pd]) enhance the practicality of this method.
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